Synthesis and evaluation of carboxymethyl chitosan for glycopeptide enrichment
Glycans are known to be involved in a variety of biological processes throughout human physiology. Mass spectrometry has demonstrated itself as powerful analytical tool for quantitative and structural characterization of glycans. Studying these molecules at the glycopeptide level however, offers dis...
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description | Glycans are known to be involved in a variety of biological processes throughout human physiology. Mass spectrometry has demonstrated itself as powerful analytical tool for quantitative and structural characterization of glycans. Studying these molecules at the glycopeptide level however, offers distinct advantages, namely the ability to characterize both the glycan and peptide fragments simultaneously, and moreover the ability to assign site specific heterogeneity. In light of this, peptides often dominate the spectrum and hinder the ionization efficiency of glycopeptides. For this reason, enrichment protocols prior to downstream MS analysis need to be developed. Here, we discuss the synthesis and use of carboxymethyl chitosan (CMCH) to enrich glycopeptides from a 12 protein mixture for MS analysis. This protocol was compared to a commercially available glycopeptide enrichment kit offered by EMD Millipore through the use of tandem mass tags (TMT) for relative quantification. Using this approach, we identified 98 unique N-linked glycopeptides and observed, that CMCH was able to enrich more sialylation than the commercial kit. In addition, we observed a trend based on TMT reporter ratios with respect to increasing sialylation. This corroborated that this stationary phase was exhibiting a mixed-mode enrichment through both hydrophilic interaction liquid chromatography (HILIC) and weak anion exchange (WAX) principles.
[Display omitted]
•Synthesis of carboxymethyl chitosan (CMCH) as a pull-down stationary phase.•Use of CMCH to enrich glycopeptides from a 12 protein mixture for MS analysis.•Compared to a commercially available glycopeptide enrichment kit.•Use of tandem mass tags (TMT) for relative quantitative comparison.•CMCH able to enrich more sialylation than the commercial kit. |
doi_str_mv | 10.1016/j.aca.2015.08.004 |
format | Article |
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[Display omitted]
•Synthesis of carboxymethyl chitosan (CMCH) as a pull-down stationary phase.•Use of CMCH to enrich glycopeptides from a 12 protein mixture for MS analysis.•Compared to a commercially available glycopeptide enrichment kit.•Use of tandem mass tags (TMT) for relative quantitative comparison.•CMCH able to enrich more sialylation than the commercial kit.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2015.08.004</identifier><identifier>PMID: 26388377</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Cattle ; Chickens ; Chitosan - analogs & derivatives ; Chitosan - chemical synthesis ; Chitosan - chemistry ; Glycopeptide ; Glycopeptides - analysis ; Glycopeptides - isolation & purification ; Horses ; Humans ; Hydrophilic interaction ; Mass spectrometry ; Molecular Sequence Data ; Proteins - chemistry ; Sialylation ; Tandem Mass Spectrometry - methods ; Tandem mass tag ; Weak anion exchange</subject><ispartof>Analytica chimica acta, 2015-09, Vol.891, p.179-189</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-e92f8ddd7f16008ae9a60b2cc065209ad0de3e7a955ab171fb99a34ed05c4bbf3</citedby><cites>FETCH-LOGICAL-c489t-e92f8ddd7f16008ae9a60b2cc065209ad0de3e7a955ab171fb99a34ed05c4bbf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.aca.2015.08.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26388377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bodnar, Edward D.</creatorcontrib><creatorcontrib>Perreault, Hélène</creatorcontrib><title>Synthesis and evaluation of carboxymethyl chitosan for glycopeptide enrichment</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><description>Glycans are known to be involved in a variety of biological processes throughout human physiology. Mass spectrometry has demonstrated itself as powerful analytical tool for quantitative and structural characterization of glycans. Studying these molecules at the glycopeptide level however, offers distinct advantages, namely the ability to characterize both the glycan and peptide fragments simultaneously, and moreover the ability to assign site specific heterogeneity. In light of this, peptides often dominate the spectrum and hinder the ionization efficiency of glycopeptides. For this reason, enrichment protocols prior to downstream MS analysis need to be developed. Here, we discuss the synthesis and use of carboxymethyl chitosan (CMCH) to enrich glycopeptides from a 12 protein mixture for MS analysis. This protocol was compared to a commercially available glycopeptide enrichment kit offered by EMD Millipore through the use of tandem mass tags (TMT) for relative quantification. Using this approach, we identified 98 unique N-linked glycopeptides and observed, that CMCH was able to enrich more sialylation than the commercial kit. In addition, we observed a trend based on TMT reporter ratios with respect to increasing sialylation. This corroborated that this stationary phase was exhibiting a mixed-mode enrichment through both hydrophilic interaction liquid chromatography (HILIC) and weak anion exchange (WAX) principles.
[Display omitted]
•Synthesis of carboxymethyl chitosan (CMCH) as a pull-down stationary phase.•Use of CMCH to enrich glycopeptides from a 12 protein mixture for MS analysis.•Compared to a commercially available glycopeptide enrichment kit.•Use of tandem mass tags (TMT) for relative quantitative comparison.•CMCH able to enrich more sialylation than the commercial kit.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Cattle</subject><subject>Chickens</subject><subject>Chitosan - analogs & derivatives</subject><subject>Chitosan - chemical synthesis</subject><subject>Chitosan - chemistry</subject><subject>Glycopeptide</subject><subject>Glycopeptides - analysis</subject><subject>Glycopeptides - isolation & purification</subject><subject>Horses</subject><subject>Humans</subject><subject>Hydrophilic interaction</subject><subject>Mass spectrometry</subject><subject>Molecular Sequence Data</subject><subject>Proteins - chemistry</subject><subject>Sialylation</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Tandem mass tag</subject><subject>Weak anion exchange</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAWxQlmwSxnk4iVihipdUwQJYW449Ia6SONhuRf6eVC0sWY2udO6V5hBySSGiQNnNOhJSRDHQLIIiAkiPyJwWeRKmSZwekzkAJGHMcpiRM-fWU4wppKdkFrOkKJI8n5OXt7H3DTrtAtGrALei3QivTR-YOpDCVuZ77NA3YxvIRnvjRB_Uxgaf7SjNgIPXCgPsrZZNh70_Jye1aB1eHO6CfDzcvy-fwtXr4_PybhXKtCh9iGVcF0qpvKYMoBBYCgZVLCWwLIZSKFCYYC7KLBMVzWldlaVIUlSQybSq6mRBrve7gzVfG3Sed9pJbFvRo9k4PnUyxigAm1C6R6U1zlms-WB1J-zIKfCdRr7mk0a-08ih4JPGqXN1mN9UHaq_xq-3CbjdAzg9udVouZMae4lKW5SeK6P_mf8BeqiEbA</recordid><startdate>20150903</startdate><enddate>20150903</enddate><creator>Bodnar, Edward D.</creator><creator>Perreault, Hélène</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150903</creationdate><title>Synthesis and evaluation of carboxymethyl chitosan for glycopeptide enrichment</title><author>Bodnar, Edward D. ; Perreault, Hélène</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-e92f8ddd7f16008ae9a60b2cc065209ad0de3e7a955ab171fb99a34ed05c4bbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Cattle</topic><topic>Chickens</topic><topic>Chitosan - analogs & derivatives</topic><topic>Chitosan - chemical synthesis</topic><topic>Chitosan - chemistry</topic><topic>Glycopeptide</topic><topic>Glycopeptides - analysis</topic><topic>Glycopeptides - isolation & purification</topic><topic>Horses</topic><topic>Humans</topic><topic>Hydrophilic interaction</topic><topic>Mass spectrometry</topic><topic>Molecular Sequence Data</topic><topic>Proteins - chemistry</topic><topic>Sialylation</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Tandem mass tag</topic><topic>Weak anion exchange</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bodnar, Edward D.</creatorcontrib><creatorcontrib>Perreault, Hélène</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bodnar, Edward D.</au><au>Perreault, Hélène</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and evaluation of carboxymethyl chitosan for glycopeptide enrichment</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2015-09-03</date><risdate>2015</risdate><volume>891</volume><spage>179</spage><epage>189</epage><pages>179-189</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>Glycans are known to be involved in a variety of biological processes throughout human physiology. Mass spectrometry has demonstrated itself as powerful analytical tool for quantitative and structural characterization of glycans. Studying these molecules at the glycopeptide level however, offers distinct advantages, namely the ability to characterize both the glycan and peptide fragments simultaneously, and moreover the ability to assign site specific heterogeneity. In light of this, peptides often dominate the spectrum and hinder the ionization efficiency of glycopeptides. For this reason, enrichment protocols prior to downstream MS analysis need to be developed. Here, we discuss the synthesis and use of carboxymethyl chitosan (CMCH) to enrich glycopeptides from a 12 protein mixture for MS analysis. This protocol was compared to a commercially available glycopeptide enrichment kit offered by EMD Millipore through the use of tandem mass tags (TMT) for relative quantification. Using this approach, we identified 98 unique N-linked glycopeptides and observed, that CMCH was able to enrich more sialylation than the commercial kit. In addition, we observed a trend based on TMT reporter ratios with respect to increasing sialylation. This corroborated that this stationary phase was exhibiting a mixed-mode enrichment through both hydrophilic interaction liquid chromatography (HILIC) and weak anion exchange (WAX) principles.
[Display omitted]
•Synthesis of carboxymethyl chitosan (CMCH) as a pull-down stationary phase.•Use of CMCH to enrich glycopeptides from a 12 protein mixture for MS analysis.•Compared to a commercially available glycopeptide enrichment kit.•Use of tandem mass tags (TMT) for relative quantitative comparison.•CMCH able to enrich more sialylation than the commercial kit.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26388377</pmid><doi>10.1016/j.aca.2015.08.004</doi><tpages>11</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Cattle Chickens Chitosan - analogs & derivatives Chitosan - chemical synthesis Chitosan - chemistry Glycopeptide Glycopeptides - analysis Glycopeptides - isolation & purification Horses Humans Hydrophilic interaction Mass spectrometry Molecular Sequence Data Proteins - chemistry Sialylation Tandem Mass Spectrometry - methods Tandem mass tag Weak anion exchange |
title | Synthesis and evaluation of carboxymethyl chitosan for glycopeptide enrichment |
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